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Diverse Shapes (diverse + shape)

Distribution by Scientific Domains

Chemistry	50%
Life Sciences	33%

Selected Abstracts

From Trifluoroacetate Complex Precursors to Monodisperse Rare-Earth Fluoride and Oxyfluoride Nanocrystals with Diverse Shapes through Controlled Fluorination in Solution Phase

CHEMISTRY - A EUROPEAN JOURNAL, Issue 8 2007
Xiao Sun
Abstract We report the first systematic synthesis of monodisperse rare-earth (RE=La to Lu, Y) fluoride and oxyfluoride nanocrystals with diverse shapes (trigonal REF3 triangular, truncated-triangular, hexagonal, and polygonal nanoplates; orthorhombic REF3 quadrilateral and zigzag-shaped nanoplates; cubic REOF nanopolyhedra and nanorods) from single-source precursors (SSP) of [RE(CF3COO)3] through controlled fluorination in oleic acid (OA)/oleylamine (OM)/1-octadecene (ODE). To selectively obtain REF3 or REOF nanocrystals, the fluorination of the REO bond to the REF bond at the nucleation stage was controlled by finely tuning the ratio of OA/ODE or OA/OM, and the reaction temperature. For phase-pure REF3 or REOF naocrystals, their shape-selective syntheses could be realized by further modifying the reaction conditions. The two-dimensional growth of the REF3 nanoplates and the one-dimensional growth of the REOF nanorods were likely due to the selective adsorption of the capping ligands on specific crystal planes of the nanocrystals. Those well-shaped nanocrystals with diverse geometric symmetries (such as D3h, D6h, C2h, Oh, and Dnh) displayed a remarkable capability to form self-assembled superlattices. By manipulating the solvent,substrate combination, the plate-shaped REF3 nanocrystals could form highly ordered nanoarrays by means of either the face-to-face formation or the edge-to-edge formation. By using this SSP strategy, we also obtained high-quality LaF3:Eu and LaF3:Eu/LaF3 triangular nanoplates that showed photoluminescent red emissions of Eu3+ ions sensitive to the surface effect. [source]

Why are species' body size distributions usually skewed to the right?

FUNCTIONAL ECOLOGY, Issue 4 2002
Jan Koz, owski
Summary 1.,Species' body size distributions are right-skewed, symmetric or left-skewed, but right-skewness strongly prevails. 2.,Skewness changes with taxonomic level, with a tendency to high right-skewness in classes and diverse skewness in orders within a class. Where the number of lower taxa allows for analysis, skewness coefficients have normal distributions, with the majority of taxa being right-skewed. 3.,Skewness changes with geographical scale. For a broad range, distributions in a class are usually right-skewed. For a narrower scale, distributions remain right-skewed or become symmetric or even close to uniform. 4.,The prevailing right-skewness of species' body size distributions is explained with macroevolutionary models, the fractal character of the environment, or body size optimization. 5.,Macroevolutionary models assume either size-biased speciation and extinction, or the existence of a constraint on small size. Macroevolutionary mechanisms seem insufficient to explain the pattern of species' body size distributions, but they may operate together with other mechanisms. 6.,Optimization models assume that directional and then stabilizing selection works after speciation events. There are two kinds of optimization approaches to study species' body size distributions. Under the first approach, it is assumed that a single energetic optimum exists for an entire taxon, and that species are distributed around this optimum. Under the second approach, each species has a separate optimum, and the species' body size distribution reflects the distribution of optimal values. 7.,Because not only energetic properties but also mortality are important in determining optimal sizes, only the second approach, that is, seeking the distribution of optimal values, seems appropriate in the context of life-history evolution. This approach predicts diverse shapes of body size distributions, with right-skewness prevailing. [source]

1D and 3D Ionic Liquid,Aluminum Hydroxide Hybrids Prepared via an Ionothermal Process,

ADVANCED FUNCTIONAL MATERIALS, Issue 14 2007
S. Park
Abstract Room-temperature ionic liquids (RTILs) are used as hierarchically multifunctional components by employing them not only as templates and co-solvents for fabricating nanostructured materials but also proton conductors for electrochemical devices. RTIL/aluminum hydroxide (RTIL,Al) hybrids containing various nanometer-sized shapes, including 1D nanorods with hexagonal tips, straight and curved nanofibers, nanofibers embedded in a porous network, and 3D octahedral-, polyhedral-, and angular spherical shapes are synthesized via a one-pot ionothermal process. The structures or shapes of the RTIL,Al hybrids are related to the anionic moieties, alkyl chain length of the RTILs, and the humidity during fabrication. In particular, the introduction of water molecules into the interface led to 3D isotropic growth of the hybrids by influencing intermolecular interactions between the RTILs and the building blocks. The shapes of the nanohybrids fabricated from RTILs containing short alkyl chains were dependent on the types of anions and on the level of humidity. These results indicate that the cooperative interactions between RTILs and aluminum hydroxides induces emerging shape-controlled hybrids. The shape-controlled nanohybrids show enhanced electrochemical properties compared to those of a conventional hybrid prepared by mixing RTILs and aluminum hydroxides, exhibiting tenfold or higher proton conductivity under anhydrous condition and thermal stability as a result of the continuous proton conduction channel and the one-pot-assembled nanoconfinement. This method is expected to be a useful technique for controlling the diverse shapes of nanometer-sized crystalline inorganic materials for a variety of applications, such as fuel cells, solar cells, rechargeable batteries, and biosensors. [source]

Multiple diverse ligands binding at a single protein site: A matter of pre-existing populations

PROTEIN SCIENCE, Issue 2 2002
Buyong Ma
Abstract Here, we comment on the steadily increasing body of data showing that proteins with specificity actually bind ligands of diverse shapes, sizes, and composition. Such a phenomenon is not surprising when one considers that binding is a dynamic process with populations in equilibrium and that the shape of the binding site is strongly influenced by the molecular partner. It derives implicitly from the concept of populations. All proteins, specific and nonspecific, exist in ensembles of substates. If the library of ligands in solution is large enough, favorably matching ligands with altered shapes and sizes can be expected to bind, with a redistribution of the protein populations. Point mutations at spatially distant sites may exert large conformational rearrangements and hinge effects, consistent with mutations away from the binding site leading to population shifts and (cross-)drug resistance. A similar effect is observed in protein superfamilies, in which different sequences with similar topologies display similar large-scale dynamic motions. The hinges are frequently at analogous sites, yet with different substrate specificity. Similar topologies yield similar conformational isomers, although with different distributions of population times, owing to the change in the conditions, that is, the change in the sequences. In turn, different distributions relate to binding of different sizes and shapes. Hence, the binding site shape and size are defined by the ligand. They are not independent entities of fixed proportions and cannot be analyzed independently of the binding partner. Such a proposition derives from viewing proteins as dynamic distributions, presenting to the incoming ligands a range of binding site shapes. It illustrates how presumably specific binding molecules can bind multiple ligands. In terms of drug design, the ability of a single receptor to recognize many dissimilar ligands shows the need to consider more diverse molecules. It provides a rationale for higher affinity inhibitors that are not derived from substrates at their transition states and indicates flexible docking schemes. [source]

The ischial callosities of Sulawesi macaques

AMERICAN JOURNAL OF PRIMATOLOGY, Issue 12 2009
Berry Juliandi
Abstract Sulawesi island has a high level of endemism, including the seven species of monkey from the genus Macaca (macaques). These monkeys have a pair of sitting pads, termed ischial callosities that have diverse shapes and previously were described verbally only. Although useful, these verbal descriptions cannot fully describe shape variation and are somewhat subjective, and cannot directly be used to analyze relationships among species. Here, we report a quantitative analysis of shape of Sulawesi macaque ischial callosities using geometric morphometric tools to optimally describe shape variation and objectively reconstruct general pattern of callosity shapes. By quantification of shape variation, we compare the relationships of each Sulawesi macaque species with each other and with the two geographically neighboring macaque species, M. nemestrina and M. fascicularis, by consensus coordinates of the callosity outlines. The Sulawesi macaques have a wider degree of variation compared with M. fascicularis and M. nemestrina; variation exists in the dorsal part and in the bending of the callosity. There are three general types of callosity shape in Sulawesi macaques: oval without bending (M. tonkeana and M. maurus), oval with outward bending (M. ochreata and M. brunnescens), and oval or reniform with inward bending (M. hecki, M. nigrescens, and M. nigra). These types are congruent with their geographical distribution. The pathway of shape change may have started from oval without bending in the center and the southern peninsula, to outward bending in the southeastern species, and to oval or reniform with inward bending in the northern species. Am. J. Primatol. 71:1021,1031, 2009. © 2009 Wiley-Liss, Inc. [source]

From Trifluoroacetate Complex Precursors to Monodisperse Rare-Earth Fluoride and Oxyfluoride Nanocrystals with Diverse Shapes through Controlled Fluorination in Solution Phase